Yuno II Mobile Operating Table — Class II medical device recall Z-0133-2021

Terminated recall by Maquet Cardiovascular Us Sales, Llc, reported 2020-10-28, distributed nationwide. Plastic socket of the IEC 60320-1 socket pulled out of the metal cage and electronic parts exposed; where the

Recall number	`Z-0133-2021`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Maquet Cardiovascular Us Sales, Llc, Wayne, NJ, United States
Recall initiated	2020-09-24
Classified	2020-10-20
Reported by FDA	2020-10-28
Terminated	2023-02-28
Distributed	Nationwide (US)
Countries outside the US	AE, AR, AU, BG, BH, BO, BR, CA, CH, CL, CN, CO, CR, CZ, DE, ES, FI, FR, GB, HK, HR, HU, ID, IL, IN, IQ, IT, JP, KE, KR, KW, LB, LV, MX, MY, NZ, OM, PL, QA, RO, RS, SA, SE, SG, TR, ZA
Quantity	6 units
Model numbers	`143302B0`, `143302F0`

Product

Yuno II Mobile Operating Table - Product Usage: support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Part 143302F0 (US) Part 143302B0 (OUS)

Reason for recall

Plastic socket of the IEC 60320-1 socket pulled out of the metal cage and electronic parts exposed; where the socket was pulled out and main cable is still connected to the main socket (power source), there is a risk that a user or third person may suffer an electric shock when coming in contact with the exposed electronic components

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0133-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.